CNR Institutional Research Information System

LIGUORI, MARIA
 Distribuzione geografica
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Continente #
AS - Asia 155
NA - Nord America 52
EU - Europa 30
Totale 237
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Nazione #
SG - Singapore 135
US - Stati Uniti d'America 52
IT - Italia 28
CN - Cina 16
KR - Corea 4
AT - Austria 1
DE - Germania 1
Totale 237
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Città #
Singapore 105
Santa Clara 13
Barcellona Pozzo di Gotto 8
Seoul 4
Guangzhou 3
Milan 3
Boardman 2
Novara 2
Volterra 2
Bovalino 1
Caltanissetta 1
Cernusco sul Naviglio 1
Montesilvano Marina 1
Rende 1
Vienna 1
Totale 148
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Nome #
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 27
Tay Sachs in South Italy 19
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 6
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. 6
Counting of peripheral extracellular vesicles in Multiple Sclerosis patients by an improved nanoplasmonic assay and dynamic light scattering 5
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 4
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia 4
Integrated analysis of microRNA and mRNA expression profiles reveals a complex interaction network in Attention Deficit Hyperactivity Disorder 4
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 4
Impact of individual cognitive profile on visuo-motor reorganization in relapsing-remitting multiple sclerosis 3
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 3
Treating epilepsy in Italy between XIX and XX century 3
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 3
A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY 3
The MicroRNA Centrism in the Orchestration of Neuroinflammation in Neurodegenerative Diseases. 3
Extended polymorphic and mutational analysis of the NOTCH3 gene in patients affected by leukoencephalopathy 3
Dysregulation of Gene Expressions in Multiple Sclerosis: TNFSF13B and Other Candidate Genes 3
Pharmacoepigenomics in neurodegenerative diseases 3
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 3
Serum prolactin concentrations in patients with multiple sclerosis 3
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis 3
Listening to the neurological teams for multiple sclerosis: the SMART project 3
A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis. 3
Anti-GM1antibodies are not associated with cerebral atrophy in patients with multiple sclerosis. 3
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs. 2
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 2
Sex and Gender Differences in Neurodegenerative Diseases: Challenges for Therapeutic Opportunities 2
Seeking a standardized normalization method for the quantification of microRNA expression 2
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 2
An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population 2
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 2
D678N mutation in a patient with an early-onset Alzheimer's Disease 2
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 2
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 2
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 2
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients 2
A longitudinal evaluation of cadasil progression by diffusion magnetic resonance imaging. 2
Personality predicts functional activation during working memory demand in patients with multiple sclerosis 2
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis 2
A novel mutation in FKRP gene in Italian patient with LGMD. 2
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 2
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis 2
Corrigendum: Dysregulation of micrornas and target genes networks in peripheral blood of patients with sporadic amyotrophic lateral sclerosis (Frontiers in molecular neuroscience, (2018), 11, 10.3389/fnmol.2018.00288) 2
Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis 2
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 2
HLA (A-B-C and DRB1) alleles and brain MRI changes in Multiple Sclerosis: a longitudinal study. 2
Visualizing genetic influences on Human brain function: Interactive effects of BNDF and COMT allelic variations on a spatial working memory network 2
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 2
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 2
MicroRNA and transcription factor co-regulatory network analysis: a combined bioinformatics and molecular strategy for uncovering genetic hub regulatory elements in multiple sclerosis pathogenesis 2
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosis. 2
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 2
CAV3 T78M mutation as polymorphic variant in South Italy 2
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 2
Molecular Characterization of Peripheral Extracellular Vesicles in Clinically Isolated Syndrome: Preliminary Suggestions from a Pilot Study. 2
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES: THE ROLE OF MRI IN THE NOTCH3 GENE SCREENING 2
Gene symbol: NOTCH3. Disease: CADASIL. 2
Precision Medicine in Neurodegenerative Diseases: Some Promising Tips Coming from the microRNAs' World. 2
The effects of BDNF Val(66)Met polymorphism on brain function in controls and patients with multiple sclerosis: An imaging genetic study. 1
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 1
Investigation of the relationship between anti-GM1 antibodies and brain atrophy in multiple sclerosis 1
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 1
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 1
Glutamate and multiple sclerosis. 1
HLA B*44: protective effects in MS susceptibility and MRI outcome measures 1
PROGRESSION OF MOBILITY IMPAIRMENT AND BRAIN WHITE MATTER LESION VOLUME IN THE ELDERLY: A TWO-YEAR LONGITUDINAL STUDY 1
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 1
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 1
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 1
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 1
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 1
A Predictive Model for MicroRNA Expressions in Pediatric Multiple Sclerosis Detection 1
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 1
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 1
Depression and Parkinson's disease:a neuropsychological view 1
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers. 1
Duchenne/Becker like phenotype and L276I mutation in FKRP gene 1
A Pilot Longitudinal Evaluation of MicroRNAs for Monitoring the Cognitive Impairment in Pediatric Multiple Sclerosis 1
COGNITIVE DYSFUNCTION AND QUALITY OF LIFE IN MULTIPLE SCLEROSIS DISEASE 1
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy 1
Dysregulation of MicroRNAs and Target Genes Networks in Peripheral Blood of Patients With Sporadic Amyotrophic Lateral Sclerosis 1
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes 1
Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity. 1
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 1
The effects of BDNF Val66Met polymorphism on brain function in controls and patients with multiple sclerosis: an imaging genetic study 1
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation 1
Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume. 1
Il Ruolo Della Rm Nello Screening Sul Gene Notch3: Distinguere I Soggetti Cadasil Apparentemente Sporadici Da Altre Leucoencefalopatie 1
Progression of Mobility Impairment and Brain White Matter Lesion Volume in the Elderly: a two-years longitudinal study 1
Association between miRNAs expression and cognitive performances of Pediatric Multiple Sclerosis patients: A pilot study 1
Preliminary evidence of NOS2A protective effect in patients with Relapsing-Remitting Multiple Sclerosis 1
Meta-Analysis of Differential Connectivity in Gene Co-Expression Networks in Multiple Sclerosis 1
Mutational analysis of the presenilin 2 gene in a group of Italian patients with familial Alzheimer's disease. 1
SERUM AND CSF ANTI-GM1 ANTIBODIES IN PATIENTS WITH GUILLAIN-BARRE-SYNDROME AND CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY 1
Molecular characterization of the Presenilin-2 gene in Italian patients with familial Alzheimer Disease. 1
Relapsing-remitting multiple sclerosis and protective effect of a NOS2A gene variant 1
HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe. 1
3T MRI Frequency of MS Cortical Lesions and Their Relationship with Cognitive Performance 1
Medicina di Precisione in Pediatria - Biotecnologie e applicazioni per lo sviluppo e la salute 1
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 1
Totale 234
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Categoria #
all - tutte 2.559
article - articoli 1.679
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 36
Totale 4.274
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202473 0 0 0 0 0 0 0 0 48 0 20 5
2024/2025196 9 12 175 0 0 0 0 0 0 0 0 0
Totale 269